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The Journal of Clinical Endocrinology & Metabolism Vol. 88, No. 1 450-458
Copyright © 2003 by The Endocrine Society


Original Article

mt1 Melatonin Receptor in the Primate Adrenal Gland: Inhibition of Adrenocorticotropin-Stimulated Cortisol Production by Melatonin

Claudia Torres-Farfan, Hans G. Richter, Pedro Rojas-García, Marcela Vergara, María L. Forcelledo, Luis E. Valladares, Fernando Torrealba, Guillermo J. Valenzuela and María Serón-Ferré

Departamento de Ciencias Fisiológicas (C.T.-F., H.G.R., P.R.-G., M.V., M.L.F., F.T., M.S.-F.), Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Casilla 114-D, and Unidad de Biología de la Reproducción (L.E.V.), Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Casilla 138-11, Santiago, Chile; and Department of Women’s Health (G.J.V.), Arrowhead Regional Medical Center, Colton, California 92324

Address all correspondence and requests for reprints to: María Serón-Ferré, Departamento de Ciencias Fisiológicas, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Casilla 114-D, Santiago, Chile. E-mail: mseron{at}genes.bio.puc.cl.

The pineal hormone melatonin participates in circadian, seasonal, and reproductive physiology. The presence of melatonin binding sites in human brain and peripheral tissues is well documented. However, in the mammalian adrenal gland, low-affinity melatonin binding sites have been detected only in the rat by some but not all authors. Conflicting evidence for a regulatory role of melatonin on adrenal cortisol production, prompted us to investigate this possibility in a New World primate, the capuchin monkey. Expression of melatonin receptors in the adrenal cortex was demonstrated through pharmacological characterization and autoradiographic localization of 2-[125I]iodomelatonin binding sites (dissociation constant = 96.9 ± 15 pM; maximal binding capacity = 3.8 ± 0.4 fmol/mg protein). The mt1 identity of these receptors was established by cDNA sequencing. Melatonin treatment of dispersed cells and explants from adrenal gland did not affect basal cortisol production. However, cortisol production stimulated by 100 nM ACTH was significantly inhibited by low melatonin concentrations (0.1–100 nM); this inhibitory effect was reversed by the mt1/MT2 melatonin antagonist luzindole. Melatonin also inhibited dibutyril-cAMP-stimulated cortisol production, suggesting that melatonin acts through a cAMP-independent signaling pathway. The present data demonstrate that the primate adrenal gland cortex expresses functional mt1 melatonin receptors and shows that melatonin inhibits ACTH-stimulated cortisol production.

This work was supported by Grants 2010140 and Líneas Complementarias 8980006, from Fondo Nacional de Desarrollo Científico y Tecnológico, Chile, Grant 98/LABENDO/Resource Maintenance Grant-2 from the World Health Organization, and a grant from San Bernardino Medical Foundation. C.T.-F. is a recipient of a doctoral fellowship from Dirección de Investigación de la Pontificia Universidad Católica de Chile.

Abbreviations: Bmax, Maximum binding capacity; (Bu)2cAMP, N,O'-dibutyryl cAMP; DNase, deoxyribonuclease; GTP, guanosine 5'-triphosphate; Kd, dissociation constant; mt1 and MT2, high affinity G protein-coupled melatonin receptors; SCN, suprachiasmatic nucleus.




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